HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 69100589, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Benzylpiperidine | HCID 31738 | — |
| Reactant | 2-chloro-N-(2-oxo-2,3-dihydro-1H-indol-5-yl)acetamide | HCID 53310272 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 69100589 | HCID 69100589 | 64.2% |
Reaction Steps
A mixture of 0.9 g (4 mmol) of 2-chloro-N-(2-oxo-2,3-dihydro-1H-indol-5-yl)-acetamide, 0.7 g (4 mmol) of potassium iodide, 0.6 ml (4 mmol) of triethylamine, 0.53 ml (3 mmol) of 4-benzyl-piperidine and 50 ml of acetonitrile is refluxed for 20 hours. The reaction mixture is concentrated and 30 ml of water and 30 ml of chloroform are added to the residue. The organic layer is separated and the water phase is extracted three times with 10 ml of chloroform. The combined organic layers are dried over sodium sulfate, concentrated and the residue is treated with diethylether and the precipitated crystals are filtered off to yield 0.7 g (64%) of the title compound. Melting Point: 176-180° C. (diethylether)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435744B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-2f2f2685b9c94a5885ccef5aa2246dfc |
| Source note | uspto-grants-2008_10 |